痛苦
受体
胰高血糖素样肽-1
肽
艾塞那肽
药理学
医学
内分泌学
内科学
生物
化学
糖尿病
生物化学
2型糖尿病
政治
法学
政治学
作者
Samuel J. Daniels,Cecilia Karlsson,Patrick Schrauwen,Victoria Parker
标识
DOI:10.1016/j.tem.2025.01.002
摘要
Identification of exendin-4 (a glucagon-like peptide-1 receptor agonist, GLP-1RA) in Gila monster venom may be regarded as one of the most serendipitous discoveries of recent times. GLP-1RAs are now an established therapeutic approach in type 2 diabetes (T2D), body weight management, and cardiovascular (CV) risk protection. Furthermore, there is a growing platform of evidence that GLP-1RA has extended benefit in renal, hepatic, respiratory, and neurological diseases. One can speculate on the biological advantage of exendin-4 to the Gila monster, but for humankind GLP-1RAs are peptides with significant potential to improve disease-related outcomes. We report on the latest evidence and mechanisms for GLP-1RA-mediated end-organ protection that uniquely highlight its future development potential across multiple disease areas.
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